rs587779013

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;GA)	6	Lynch syndrome, pathogenic mutation

Make rs587779013(GA;GA)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

36993587

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs587779013
dbSNP (classic)	rs587779013
ClinGen	rs587779013
ebi	rs587779013
HLI	rs587779013
Exac	rs587779013
Gnomad	rs587779013
Varsome	rs587779013
LitVar	rs587779013
Map	rs587779013
PheGenI	rs587779013
Biobank	rs587779013
1000 genomes	rs587779013
hgdp	rs587779013
ensembl	rs587779013
geneview	rs587779013
scholar	rs587779013
google	rs587779013
pharmgkb	rs587779013
gwascentral	rs587779013
openSNP	rs587779013
23andMe	rs587779013
SNPshot	rs587779013
SNPdbe	rs587779013
MSV3d	rs587779013
GWAS Ctlg	rs587779013

Max Magnitude

6

ClinVar
Risk	rs587779013(GA;GA)
Alt	rs587779013(GA;GA)
Reference	Rs587779013(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37035077_37035078dupGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075699.2,